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CARDINAL HEALTH SLC40ELCCBRecalls & reported problems

Cardinal Health 200, LLC · STERILE EXPLORATORY LAP PACK · Class 2

Data updated Oct 18, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10887488236506), received between Sep 15, 2016 and Sep 15, 2016 — classified as 1 malfunction.

The most frequently reported specific device problem is “Insufficient Device Problem Information” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 18, 2026.

Most reported problems

Device problems

  • Insufficient Device Problem Information1

Patient problems

  • No Known Impact Or Consequence To Patient1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 15, 2016Insufficient Device Problem Information

    BASED ON THE INFORMATION FROM THE CUSTOMER THE GOWN A9040NA HAD STRIKE THROUGH ON THE SLEEVE. THE PATIENT HAD (B)(6). SEVERAL ATTEMPTS WERE MADE TO GATHER MORE INFORMATION FOR THIS REPORT, HOWEVER THE DOCTOR WOULD NOT PROVIDE ANY ADDITIONAL INFORMATION.

    Patient problems: No Known Impact Or Consequence To Patient

    MAUDE report 5952552 ↗

Other laparoscopy kit devices

All laparoscopy kit devices →

Sources and updates

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